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HPV IgM Rapid Test Device (serum)

EUDAMED

Class IVD General (EU MDR)

Ref A111701D

by Hangzhou Cybereagen Biotech Co., Ltd.

Identity

Trade Name
HPV IgM Rapid Test Device (serum) EUDAMED
Model / Reference
A111701D EUDAMED

Identifiers

Primary DI / UDI-DI
06976753472743 EUDAMED
Basic UDI-DI
B-06976753472743 EUDAMED
EMDN Code
W0105041001 HPV ANTIGEN / ANTIBODIES EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

HPV IgM Rapid Test Device (serum) by Hangzhou Cybereagen Biotech Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000037850
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED ba3269c5-d723-43c0-a3d0-b1bfcf7c44ec 61 fields · synced Jun 19, 2026